Canonical Allele Identifier: CA2639075602

Gene: RPS6KB1

Linked Data

• gnomAD v4: 17-59946934-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.59946936del , CM000679.2:g.59946936del	GRCh38
NC_000017.10:g.58024297del , CM000679.1:g.58024297del	GRCh37
NC_000017.9:g.55379079del	NCBI36
NG_029513.1:g.58855del

Transcript Alleles

HGVS	Amino-acid change
ENST00000225577.9:c.*148del MANE Select	ENSP00000225577.4:n.*148del
ENST00000225577.8:c.*148del	ENSP00000225577.4:n.*148del
ENST00000393021.7:c.*148del	ENSP00000376744.3:n.*148del
ENST00000406116.7:c.1341-651del	ENSP00000384335.3:n.1341-651del
ENST00000443572.6:c.*148del	ENSP00000441993.1:n.*148del
ENST00000472940.5:c.*1761del	ENSP00000468058.1:n.*1761del
ENST00000475155.1:n.714del
ENST00000591035.1:c.149+1418del	ENSP00000468280.1:n.149+1418del
NM_001272042.1:c.*148del	NP_001258971.1:n.*148del
NM_001272043.1:c.1341-651del	NP_001258972.1:n.1341-651del
NM_001272044.1:c.*148del	NP_001258973.1:n.*148del
NM_001272060.1:c.*148del	NP_001258989.1:n.*148del
NM_003161.3:c.*148del	NP_003152.1:n.*148del
XM_011525101.1:c.*148del	XP_011523403.1:n.*148del
XM_011525103.1:c.*148del	XP_011523405.1:n.*148del
XM_011525104.1:c.*148del	XP_011523406.1:n.*148del
XM_011525101.3:c.*148del	XP_011523403.1:n.*148del
XM_011525103.3:c.*148del	XP_011523405.1:n.*148del
XM_017024929.1:c.*148del	XP_016880418.1:n.*148del
XM_017024930.2:c.*148del	XP_016880419.1:n.*148del
XM_017024931.2:c.*148del	XP_016880420.1:n.*148del
XM_017024932.2:c.*148del	XP_016880421.1:n.*148del
XM_017024933.2:c.*148del	XP_016880422.1:n.*148del
XR_001752581.2:n.1972del
XR_001752582.2:n.1779del
XR_001752583.2:n.1671del
XR_002958051.1:n.3463del
NM_003161.4:c.*148del MANE Select	NP_003152.1:n.*148del
NM_001272043.2:c.1341-651del	NP_001258972.1:n.1341-651del
NM_001369669.1:c.*148del	NP_001356598.1:n.*148del
NM_001369670.1:c.*148del	NP_001356599.1:n.*148del
NM_001369671.1:c.*148del	NP_001356600.1:n.*148del
NM_001369672.1:c.*148del	NP_001356601.1:n.*148del
NM_001369673.1:c.*1177del	NP_001356602.1:n.*1177del
NM_001369674.1:c.*1319del	NP_001356603.1:n.*1319del
NM_001369675.1:c.*1211del	NP_001356604.1:n.*1211del
NM_001369676.1:c.*1080del	NP_001356605.1:n.*1080del
NM_001369677.1:c.*1430del	NP_001356606.1:n.*1430del
NM_001369678.1:c.*1177del	NP_001356607.1:n.*1177del
NM_001369679.1:c.*1434del	NP_001356608.1:n.*1434del
NR_161455.1:n.1642del
NR_161456.1:n.1793del
NR_161457.1:n.1689del
NR_161458.1:n.1987del
NR_161459.1:n.1768del
NR_161460.1:n.2033del
NR_161461.1:n.1794del
NR_161462.1:n.1686del
NM_001272042.2:c.*148del	NP_001258971.1:n.*148del
NM_001272044.2:c.*148del	NP_001258973.1:n.*148del
NM_001272060.2:c.*148del	NP_001258989.1:n.*148del